Canonical Allele Identifier: PA2826561919
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376571
ClinVar RCV Id: RCV000417996 RCV000417784 RCV000423257 RCV000422633 RCV000425147 RCV000426543 RCV000427160 RCV000432450 RCV000434994 RCV000433975 RCV000434565 RCV000437830 RCV000439618 RCV000442522 RCV000445223 RCV000785535 RCV001023834 RCV003621529 RCV004022204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Cys17Gly
CA16602997
NM_001276697.3:c.49T>G